Kindly find some of our project experiences below.
Program Management & Product Ownership | Life Science
Data Solutions
Manage implementation of medical device log data platform across all global business fields ensuring global data compliance in the light of MDR and GDPR
Accountable for stakeholder management at L3 and connecting all business fields | Accountable for phased planning and global rollout | Responsible for business requirement collection and technical translation | Ownership of global log data platform | Interface between portfolio management, data governance and development team
Bid and Program Management | Electronics
Commercial Excellence
Manage study and preparation for investment approval of pricing optimization and management strategies on L1
Accountable for preparing and executing request for proposal (RfP) | Accountable for budget and resource controlling < 2 Mio | Prepare decision making of L2/L3 stakeholder | Interfacing to Commercial, Marketing, Sales, Product Management, partner study in sector Life Science, and vendors
Project Management | Electronics
Surface Solutions
Manage integration of surface scanner robot into laboratory and Palantir-based advanced analytics environment, feasibility study depletion of system landscape
Accountable for budget and resource controlling < 0.5 Mio | Prepare decision making of L3 stakeholder | Interfacing to Business, Laboratory, Advanced Analytics, IT Infrastructure, IT Security, Data Privacy, Quality team and Contractors (vendor)
Bid and Project Management | Pharma
Chemical Pharmaceutical Development
Manage implementation of analytical solution for drug substance and drug product relations in the area of Analytical Development and Pharmaceutical Technologies
Responsible for preparing and executing request for proposal (RfP) | Accountable for budget and resource controlling < 0.5 Mio | Prepare decision making of L3 stakeholder | Interfacing to Business, Procurement, IT Security, Data Privacy, Quality and Validation
Bid and Project Management | Pharma
Global Scientific Exchange, Global Patient Safety, Global Biostatistics
Manage GxP-relevant implementation of a structured content authoring solution in context of a proof of concept in the area of Medical Information (GSE&C), Patient Safety (GBS) and Medical Writing (GB)
Responsible for preparing and executing request for proposal (RfP) | Accountable for budget and resource controlling < 0.5 Mio | Prepare decision making of L3 stakeholder | Interfacing to Business, Procurement, IT Security, Data Privacy, Quality and Validation
Bid and Program Management | Pharma
Global Clinical Operation, Clinical Trial Transparency
Manage GxP-relevant implementation of measures of digital outreach to patients via website and social media, partnering with pilot study in therapeutic area of neurodegenerative diseases
Manage GxP-relevant implementation of mobile app and concierge service to keep patients engaged during a clinical trial, partnering with pilot study in therapeutic area of oncology
Manage implementation of global trial finder and trial education website, see
https://clinicaltrials.merckgroup.com/en/
Manage and execute development of framework concept for implementation of global compound websites, see
https://www.clinicaltrials.targeting-met.com/en
Accountable for budget and resources < 2.0 Mio | Decision making on stakeholder L2/3
Project Management | Pharma
Quality & Manufacturing, Release & Development, Submission
Optimization and coordination with client’s program and project management for data cleaning and migration activities
Internal resource planning, forecasts and scorecards for program management in order to streamline supervision and reporting efforts
Technical Management, User Training | Pharma Legal
Manage technical team for company-wide, GxP-relevant implementation of global contract management system comprising processes and system, interface to business team
Own and manage validation activities and data migration of full legal document setup | Own and manage system availability, requirement implementation and transition into operations | Lead integration of electronic signature process and functionality
